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Drug Development

FDA clears 2 treatments for emergency bleeding

by Rowan Walrath
August 23, 2024 | A version of this story appeared in Volume 102, Issue 26

 

The US Food and Drug Administration has green-lighted two new products designed to stop severe bleeding. Cresilon’s Traumagel received 510(k) clearance, meaning the agency approved it as a new medical device. The product, a plant-based gel that comes in a syringe, is designed to be inserted at the surface of a wound to stop “all types of bleeds,” according to Brooklyn, New York–based Cresilon. Meanwhile, Octapharma’s octaplasLG Powder, a lyophilized form of blood plasma, received an emergency use authorization that specifically allows military personnel to administer it when plasma is unavailable or impractical. The powder is a freeze-dried version of Octapharma’s pooled blood plasma, octaplas, which the FDA approved in 2013.

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